4.6 Article

KSOM-R supports both mouse and rat preimplantation embryo development in vitro

Journal

THERIOGENOLOGY
Volume 198, Issue -, Pages 69-74

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.theriogenology.2022.12.024

Keywords

Embryo culture; mKSOM; mKSOM-R; Shelf life

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The modified KSOM-R with enriched amino acids showed a positive effect on rat embryo development and could be extended to support mouse embryo development. After 6 months of storage at 2-8 degrees C, the modified KSOM-R and KSOM maintained comparable developmental rates for both mouse and rat embryos. This study suggests the possibility of reducing media inventory by using the modified KSOM-R for culturing both mouse and rat embryos and the potential for creating quality media with extended shelf life through modifications.
A modified KSOM for rat embryo culture (KSOM-R), which has enriched taurine, glycine, glutamic acid, and alanine, promoted rat embryo development in vitro. Since mice and rats share similar amino acid profiles in their female reproductive tracts, this study explored whether KSOM-R would also have a positive effect on mouse embryo development and if KSOM-R modifications could extend its shelf time at 2-8 degrees C for consistency. We first examined the effects of newly made (<= 1 month at 2-8 degrees C) antibiotics -free KSOM-R (mKSOM-R), antibiotics-free KSOM (mKSOM) and KSOM on the development of in vivo or in vitro derived C57BL/6NJ zygotes. We then investigated the effect of extended shelf life (6 months at 2 -8 degrees C) of mKSOM-R and mKOSM on the development of C57BL/6NJ mouse and Sprague Dawley (SD) rat embryos. The results showed that there were no significant differences in cleavage, blastocyst, and hatching rates of C57BL/6NJ embryos among the three freshly made media. After 6 months of storage at 2 -8 degrees C, mKSOM-R and mKSOM were still able to support the development of in vivo C57BL/6NJ zygotes at comparable rates seen with newly made (<= 1 month at 2-8 degrees C) KSOM (control) in terms of cleavage, blastocyst formation and hatching. There were also no significant differences in total cell numbers in day 4 blastocysts among the three groups. After surgical embryo transfers, C57BL/6NJ blastocysts cultured in mKSOM-R (6 months at 2-8 degrees C) and newly made (<= 1 month at 2-8 degrees C) KSOM culture developed into live pups. These pups had no gross abnormalities in animal morphology and growth. SD zygotes cultured in mKSOM-R stored at 2-8 degrees C for 6 months developed at comparable rates in cleavage, blastocyst and hatching rates when compared to those cultured in newly made mKSOM-R (<= 1 month at 2-8 degrees C). The data showed that, although no significant beneficial effects were observed on mouse embryo develop-ment, mKSOM-R was able to support both mouse and rat embryo development in vitro. Additionally, mKSOM-R and mKSOM can be stored at 2-8 degrees C for at least 6 months without significantly compromising quality. This study suggests that it is possible to reduce the media inventory by using only mKSOM-R to culture both mouse and rat embryos, and quality media with extended shelf life can be made through modifications.(c) 2022 Elsevier Inc. All rights reserved.

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